43 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FIXPINE II SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131167453·ACTO, ITC P R BE
Osstell SmartPeg Type 100
FDA UDI
Osstell AB·09010522002117·ISQ Measurement Peg
CONKLUSION
FDA UDI
SIGNUS Medizintechnik GmbH·04047844013700·The CONKLUSION Pedicle Screw System is a spinal...
Ear Tip PM007 Pack/100 pcs. (Grason)
FDA UDI
PATH medical GmbH·04260223142062·PATH MEDICAL is not manufacturer or Labeler of ...
Disposable Sterile Kit
FDA UDI
RESTORATION ROBOTICS, INC.·00850470007098·
Indus®
FDA UDI
SPINEFRONTIER, INC.·00190361001447·Invue Max, Four Level ACP, 65mm
Zavation
FDA UDI
Zavation LLC·00197157002046·6.5mm Tap
UA Transfer Die
FDA UDI
BICON, LLC·00813110026897·UA6 SP-TP Transfer Dies (2)
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494464034·Grasping Forceps Straight Jaw
D 5.0mm, WL 150mm
Ear Tip PM007H Pack/100 pcs.
FDA UDI
PATH medical GmbH·04260223146862·7 mm mushroom ear tip, hard version
DIAMOND ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COULTER HMX ANALYZER, MODEL 6605523, COULTER HMX WITH AUTOLOADER, MODEL 6605526
FDA 510(k)
FDA Class 2
·Hematology
LINEAR? ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 30, 2025
UNKNOWN IV CATHETER
FDA Adverse Event
Injury
·BD (SUZHOU)·Product code FOZ·January 13, 2016
LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·May 8, 2013
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·September 12, 2014
FIXODENT ADHESIVE CREAM (CALCIUM ZINC GANTREZ SALT 44.4%, CELLULOSE GUM 20%) CRE
FDA Adverse Event
Injury
·PROCTER & GAMBLE MFG. GMBH·Product code KOO·May 19, 2011
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·May 1, 2014
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·April 28, 2014